Precision Dynamics Corp.
FDA 510(k) & PMA Approved Devices — 25 products
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Total Devices25
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K020718 | SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE | HFW | 2002-06-03 | View |
| 510(k) | K994353 | SECURELINE DISPOSABLE FETAL MONITORING STRAPS #3860 AND #3565 | HFM | 2000-03-22 | View |
| 510(k) | K994263 | SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540 | HFW | 2000-01-24 | View |
| 510(k) | K990737 | 'ECURLINE UMBILICAL CORD CLAMP #3500 | HFW | 1999-04-06 | View |
| 510(k) | K884357 | PRECISION BIOPORT COLLECTION & TRANSPORT SYSTEM | KOT | 1988-11-01 | View |
| 510(k) | K882580 | MECHANICAL CHANGE IN IN-VITRO MICRO DEVICE | JTW | 1988-07-08 | View |
| 510(k) | K874665 | SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY | LRP | 1988-01-20 | View |
| 510(k) | K873369 | SECURLINE FRANSEENE NEEDLE | KNW | 1987-10-20 | View |
| 510(k) | K872507 | PRECISION CULTURE C.A.T.S. COLLECT/TRANS HSV I/II | JSM | 1987-07-09 | View |
| 510(k) | K863164 | AGAR REDUCTION IN FORMULA FOR PDC 110 & 310 MEDIA | JSM | 1986-08-27 | View |
| 510(k) | K851364 | FRANZEN NEEDLE GUIDE FOR TRANSRECTAL PROSTATE BIOP | KNW | 1985-04-22 | View |
| 510(k) | K844634 | PDC 104 & PDC 304 STYLE CULTURE COLLECTION & TRANS | JSM | 1985-01-30 | View |
| 510(k) | K844865 | SECURLINE SURGICAL SKIN MARKER 1000 | FZZ | 1985-01-14 | View |
| 510(k) | K844369 | BBL PORT-A-CUL 21628 DOUBLE SWAB SULTURE COLLECTIO | JSM | 1985-01-04 | View |
| 510(k) | K844370 | BBL PORT-A-CUL 21627 SINGLE SWAB CULTURE COLLECT | JSM | 1985-01-04 | View |
| 510(k) | K840820 | SECURLINE SURGICAL SKIN MARKER 1000 | FZZ | 1984-04-25 | View |
| 510(k) | K830235 | FRANZEN NEEDLE GUIDE | GDM | 1983-02-23 | View |
| 510(k) | K791953 | PDC 304 DOUBLE SWAB CULTURE COLLECTION | JTW | 1979-10-30 | View |
| 510(k) | K791924 | PDC 104 SINGLE SWAB CULTURE COLLECTION | JTW | 1979-10-17 | View |
| 510(k) | K772209 | CULTURE COLLEC. TRANS. SYS., DOUBLE DRY | JTW | 1977-12-20 | View |
No matching devices.
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